Hi,

I did some more testing to see what could be the problem. The main weird
thing I see is that in the coords_for_fdt_matrix3 file, there are some
strange values:
coords_for_fdt_matrix3 :
309  -57  38  0  8341
308  -57  38  0  8342
307  -56  38  0  8343
306  -55  37  0  8344
306  -55  36  0  8345
305  -55  36  0  8346
304  -55  35  0  8347
304  -54  34  0  8348
tract_space_coords_for_fdt_matrix3:
263  -44  30  0  0
276  -40  72  0  1
311  -5  42  0  2
266  27  59  0  3
286  -90  23  0  4
313  -52  47  0  5
292  52  5  0  6


If the first 3 values are x-y-z then this is somewhere outside the brain
probably.
However, when I use the L.STS.fsl_MNI_new.asc and brainmap_filelist.txt  inputs
as seeds (-x ) without any matrix options, the outputs (as in
fdt_paths.nii.gz) look like expected. So this would indicate that there is
no problem in transforming the seeds to dti space and reading them I would
think?

Any suggestions?

-Maarten


On Mon, Jul 20, 2015 at 6:29 PM, Maarten Vaessen <[email protected]>
wrote:

> Ah, of course!
> That is:
>
> wb_command -probtrackx-dot-convert fdt_matrix3.dot
> test_dot_to_cifti.dconn.nii -col-surface L.STS.func.gii -row-cifti
> 91282_Greyordinates.dscalar.nii COLUMN -transpose
>
> On Mon, Jul 20, 2015 at 5:54 PM, Glasser, Matthew <[email protected]
> > wrote:
>
>>  No I meant the dot convert.
>>
>>  Matt.
>>
>>   From: Maarten Vaessen <[email protected]>
>> Date: Monday, July 20, 2015 at 3:29 AM
>> To: Matt Glasser <[email protected]>
>> Cc: "[email protected]" <[email protected]>
>> Subject: Re: [HCP-Users] tractography
>>
>>   The conversion was done like this:
>>
>>  wb_command -gifti-label-to-roi
>> ../../MNINonLinear/fsaverage_LR32k/102816.L.aparc.a2009s.32k_fs_LR.label.gii
>> L.STS.func.gii -name S_temporal_sup
>> surf2surf  -i
>> ../../MNINonLinear/fsaverage_LR32k/102816.L.white.32k_fs_LR.surf.gii -o
>> L.STS.fsl_MNI_new.asc --outputtype=ASCII  --values=L.STS.func.gii
>>
>>  Is this what you were referring to?
>>
>>  -Maarten
>>
>> On Sun, Jul 19, 2015 at 10:20 PM, Glasser, Matthew <
>> [email protected]> wrote:
>>
>>>  The --onewaycondition flag doesn’t seem sensible with matrix3.  Also I
>>> don’t know what your command was for doing the conversion.  Here is the
>>> probtrackx2 call that didn’t make it onto the list:
>>>
>>>  probtrackx2 -x L.STS.fsl_MNI_new.asc --onewaycondition --omatrix3
>>> --target3=L.STS.fsl_MNI_new.asc
>>> --lrtarget3=brainmap_HCP/brainmap_filelist.txt -P 100 --forcedir
>>> --dir=./test_surf_track_STS_brainmap_seedspace -s
>>> ../Diffusion.bedpostX/merged -m nodif_brain_mask.nii.gz
>>> --seedref=../../MNINonLinear/T1w_restore.nii.gz -V 2 --opd --pd
>>> --distthresh3=2 --xfm=../../MNINonLinear/xfms/standard2acpc_dc.nii.gz
>>> --invxfm=../../MNINonLinear/xfms/acpc_dc2standard.nii.gz
>>>
>>>
>>>  Peace,
>>>
>>>
>>>  Matt.
>>>
>>>   From: Maarten Vaessen <[email protected]>
>>> Date: Sunday, July 19, 2015 at 12:03 PM
>>> To: Matt Glasser <[email protected]>
>>> Cc: "[email protected]" <[email protected]>
>>> Subject: Re: FW: [HCP-Users] tractography
>>>
>>>   In this case: seed region to whole brain connectivity. The STS seed
>>> is mainly for testing purposes (not as many seed points as the whole WM),
>>> the final analysis will use all WM voxels as seeds though. In fact,when I
>>> run the analysis with WM as the seed the results look equally strange: only
>>> connectivity to what appears to be the right inferior posterior cortex.
>>> Could this be an issue with the seed-space to dti-space parameters?
>>>
>>>  -M
>>>
>>> On Sun, Jul 19, 2015 at 5:31 PM, Glasser, Matthew <
>>> [email protected]> wrote:
>>>
>>>>  What is it that you are trying to achieve?  Usually one uses a seed
>>>> of all white matter voxels with matrix3.
>>>>
>>>>  Peace,
>>>>
>>>>  Matt.
>>>>
>>>>   From: Maarten Vaessen <[email protected]>
>>>> Date: Sunday, July 19, 2015 at 3:41 AM
>>>> To: Matt Glasser <[email protected]>
>>>> Subject: Re: [HCP-Users] tractography
>>>>
>>>>   Hi Matthew,
>>>>
>>>>  I tried to use the file you suggested, and I can convert the .dot
>>>> without problem. However, the results don't make any sense, so I think
>>>> there might be something wrong in my processing pipeline. Would you mind
>>>> having a quick look at it and see if I do something wrong?
>>>> Attached is the pipeline and a screenshot from the matrix as loaded in
>>>> MATLAB.
>>>> As you can see from the screenshot, there is only very limited number
>>>> of none zeros. And weirdest of all, they appear at column indices which are
>>>> probably somewhere in the right hemisphere (seed is in the left).
>>>>
>>>>  Thanks,
>>>>
>>>>  -Maarten
>>>>
>>>> On Wed, Jul 15, 2015 at 6:20 PM, Glasser, Matthew <
>>>> [email protected]> wrote:
>>>>
>>>>>  You should be able to use this file:
>>>>>
>>>>>
>>>>> https://github.com/Washington-University/Pipelines/blob/master/global/templates/91282_Greyordinates/91282_Greyordinates.dscalar.nii
>>>>>
>>>>>  Peace,
>>>>>
>>>>>  Matt.
>>>>>
>>>>>   From: <[email protected]> on behalf of Maarten
>>>>> Vaessen <[email protected]>
>>>>> Date: Wednesday, July 15, 2015 at 4:44 AM
>>>>> To: "[email protected]" <[email protected]>
>>>>> Subject: Re: [HCP-Users] tractography
>>>>>
>>>>>   Hello,
>>>>>
>>>>>
>>>>> I followed the guide lines below to create a dense connectome with 
>>>>> probtrackx. I was just wondering how to proceed with converting the .dot 
>>>>> file from probtrackx to cifti using wb_command -probtrackx-dot-convert 
>>>>> (for visualisation in wb_view). Specifically, what cifti file can I use 
>>>>> as input for the -row-cifti option? So, what files released with the HCP 
>>>>> data contain the correct brainmap?
>>>>>
>>>>>
>>>>> Thx
>>>>>
>>>>>
>>>>> -Maarten
>>>>>
>>>>>
>>>>>
>>>>>
>>>>>
>>>>> _______________________________________________________________
>>>>>
>>>>> Hi
>>>>>
>>>>> You need to create such a file that contains the 90k grayordinates. To 
>>>>> ensure
>>>>> consistency we do that in MNI 2mm space:
>>>>>
>>>>> - First create surface files in an FSL friendly format. Use the 32k 
>>>>> surfaces,
>>>>> as the vertices are ~2mm apart.
>>>>> Left Surface:
>>>>> surf2surf -i
>>>>> $Subject/MNINonLinear/fsaverage_LR32k/${Subject}.L.white.32k_fs_LR.surf.gii
>>>>>  -o
>>>>> white.L.asc --outputtype=ASCII
>>>>> --values=$Subject/MNINonLinear/fsaverage_LR32k//${Subject}.L.atlasroi.32k_fs_LR.shape.gii
>>>>>
>>>>> Right Surface:
>>>>> surf2surf -i
>>>>> $Subject/MNINonLinear/fsaverage_LR32k/${Subject}.R.white.32k_fs_LR.surf.gii
>>>>>  -o
>>>>> white.R.asc --outputtype=ASCII
>>>>> --values=$Subject/MNINonLinear/fsaverage_LR32k//${Subject}.R.atlasroi.32k_fs_LR.shape.gii
>>>>>
>>>>> - Then extract the volume subcortical files from e.g.
>>>>> $Subject/MNINonLinear/ROIs/Atlas_Rois.2.nii.gz, let’s say as
>>>>> CIFTI_Structure_{Name}.nii.gz, using e.g. fslmaths or your favourite tool 
>>>>> for
>>>>> ROI extraction. You should get 19 of these NIFTI files. (You can 
>>>>> obviously use
>>>>> your favourite subcortical parcellation here, but if you want consistency 
>>>>> with
>>>>> the CIFTI standard grayordinates, you need to resample the final results, 
>>>>> the
>>>>> file above ensures consistency).
>>>>>
>>>>> - Put all the filenames in a text file in the following sequence, to 
>>>>> ensure
>>>>> consistency with the rest of the CIFTIs:
>>>>>
>>>>> white.L.asc
>>>>> white.R.asc
>>>>> CIFTI_STRUCTURE_ACCUMBENS_LEFT.nii.gz
>>>>> CIFTI_STRUCTURE_ACCUMBENS_RIGHT.nii.gz
>>>>> CIFTI_STRUCTURE_AMYGDALA_LEFT.nii.gz
>>>>> CIFTI_STRUCTURE_AMYGDALA_RIGHT.nii.gz
>>>>> CIFTI_STRUCTURE_BRAIN_STEM.nii.gz
>>>>> CIFTI_STRUCTURE_CAUDATE_LEFT.nii.gz
>>>>> CIFTI_STRUCTURE_CAUDATE_RIGHT.nii.gz
>>>>> CIFTI_STRUCTURE_CEREBELLUM_LEFT.nii.gz
>>>>> CIFTI_STRUCTURE_CEREBELLUM_RIGHT.nii.gz
>>>>> CIFTI_STRUCTURE_DIENCEPHALON_VENTRAL_LEFT.nii.gz
>>>>> CIFTI_STRUCTURE_DIENCEPHALON_VENTRAL_RIGHT.nii.gz
>>>>> CIFTI_STRUCTURE_HIPPOCAMPUS_LEFT.nii.gz
>>>>> CIFTI_STRUCTURE_HIPPOCAMPUS_RIGHT.nii.gz
>>>>> CIFTI_STRUCTURE_PALLIDUM_LEFT.nii.gz
>>>>> CIFTI_STRUCTURE_PALLIDUM_RIGHT.nii.gz
>>>>> CIFTI_STRUCTURE_PUTAMEN_LEFT.nii.gz
>>>>> CIFTI_STRUCTURE_PUTAMEN_RIGHT.nii.gz
>>>>> CIFTI_STRUCTURE_THALAMUS_LEFT.nii.gz
>>>>> CIFTI_STRUCTURE_THALAMUS_RIGHT.nii.gz
>>>>>
>>>>>
>>>>> - You can then use such a file in FSL probtrackx2 as a seed (for Matrix1) 
>>>>> or as
>>>>> a target3 (for Matrix3). Notice that running a single probtrackx2 command 
>>>>> with
>>>>> all these seed locations and with many samples per location will require 
>>>>> huge
>>>>> processing power and memory. In practice, we run multiple probtrackx2 in
>>>>> parallel, by splitting and parallelising the computation by using the 
>>>>> --rseed
>>>>> option in probtrackx2 and using a small number of samples --nsamples per
>>>>> instance. I.e. instead of running one command, which will attempt to 
>>>>> propagate
>>>>> 5000 curves per seed, we can run e.g. 100 instances of the above commands,
>>>>> using --nsamples=50 and --rseed=i, i=1..100. Results can then be combined 
>>>>> using
>>>>> fdt_matrix_merge (which however also needs quite a lot of memory to 
>>>>> produce the
>>>>> final dense connectomes, but at least it is one final process).
>>>>>
>>>>> - Another approach for parallelisation would be to split the seed 
>>>>> locations and
>>>>> merge the final matrices. There is no solution that fits all systems, you
>>>>> should try and find the best approach depending on your computing 
>>>>> resources.
>>>>>
>>>>> Hope this helps
>>>>> Stam
>>>>>
>>>>>
>>>>>
>>>>>
>>>>>
>>>>> On 19 May 2015, at 01:01, David R. Haynor 
>>>>> <[email protected]<mailto:[email protected] <[email protected]>>>
>>>>> wrote:
>>>>>
>>>>> hi HCP,
>>>>>
>>>>> we are trying to do tractography using FSL and HCP data.  i have some 
>>>>> questions
>>>>> -- i suspect they have been answered already, but couldn't find those 
>>>>> answers:
>>>>>
>>>>> 1. is there a file containing the grayordinate coordinates in the 
>>>>> diffusion
>>>>> space for a particular subject, both subcortical voxels and cortical 
>>>>> vertices?
>>>>>
>>>>> 2. if i want to use some cortical and subcortical voxels from the list of
>>>>> grayordinates as targets, do i have to run probtrackx2 twice (i.e. once 
>>>>> for the
>>>>> cortical surface vertices and once for the subcortical voxels), or can i 
>>>>> run it
>>>>> just once?
>>>>>
>>>>> 3. where is the label file for the grayordinate vertices/voxels for a 
>>>>> given
>>>>> subject?
>>>>>
>>>>> thanks in advance.
>>>>>
>>>>> -dh
>>>>> _______________________________________________
>>>>> HCP-Users mailing 
>>>>> [email protected]<mailto:[email protected] 
>>>>> <[email protected]>>http://lists.humanconnectome.org/mailman/listinfo/hcp-users
>>>>>
>>>>>
>>>>> _______________________________________________
>>>>> HCP-Users mailing 
>>>>> [email protected]http://lists.humanconnectome.org/mailman/listinfo/hcp-users
>>>>>
>>>>>  _______________________________________________
>>>>> HCP-Users mailing list
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>>>>>
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